Article

A case of 17q12 deletion syndrome characterized by hypokalemia and hypomagnesemia

2023-12-26

Abstract excerpt

<h4>Background: </h4> The 17q12 deletion syndrome is a rare autosomal dominant disease, the phenotypes of genetic diseases include abnormalities of the kidney, pancreas, brain, gastrointestinal tract, and reproductive tract. The manifestations of these diseases vary among individuals, and the clinical manifestations are different. Here we report a case of 17q12 deletion syndrome characterized by hypokalemia and hy...

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Literature Corpus work: 3c03d736-63d8-58cf-b1d5-61582cc1e2ad
DOI: 10.21203/rs.3.rs-3755758/v1

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